Location: London.
Contract: Full Time.
Responsibilities
- Development of regulatory documentation and timely submissions to regulatory authorities.
- Manage and conduct communications with external regulatory authorities and ensure positive and trusted relationships are developed.
- Ensure regulatory plans are established and followed to support future pharmaceutical licensing applications.
- Work collaboratively to ensure robust studies are planned and carried out to the required regulatory standards.
Requirements
- BSc or advanced degree in any relevant scientific field.
- Prior regulatory affairs experience in pharmaceutical development.
- Good knowledge of clinical trial regulations.
- Ability to multitask and prioritize.
- Prepare and manage clinical trial applications.
- Interpersonal and communication skills.
- Proofreading, editing, and technical system skills.
I am looking forward to having a chat with you if you are suitable for this role. For more information on this exciting opportunity please email a copy of your CV in MS WORD format to cv@specialistmedics.com using Regulatory Affairs Specialist as the Subject.
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Job Category: Doctors
Job Location: London